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噬菌体免疫沉淀测序(PhIP-Seq):高通量血清学的前景

Phage ImmunoPrecipitation Sequencing (PhIP-Seq): The Promise of High Throughput Serology.

作者信息

Tiu Charles Kevin, Zhu Feng, Wang Lin-Fa, de Alwis Ruklanthi

机构信息

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore 169857, Singapore.

SingHealth Duke-NUS Global Health Institute, Singapore 169857, Singapore.

出版信息

Pathogens. 2022 May 11;11(5):568. doi: 10.3390/pathogens11050568.

DOI:10.3390/pathogens11050568
PMID:35631089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9143919/
Abstract

Phage ImmunoPrecipitation Sequencing (PhIP-Seq) is a high throughput serological technology that is revolutionizing the manner in which we track antibody profiles. In this review, we mainly focus on its application to viral infectious diseases. Through the pull-down of patient antibodies using peptide-tile-expressing T7 bacteriophages and detection using next-generation sequencing (NGS), PhIP-Seq allows the determination of antibody repertoires against peptide targets from hundreds of proteins and pathogens. It differs from conventional serological techniques in that PhIP-Seq does not require protein expression and purification. It also allows for the testing of many samples against the whole virome. PhIP-Seq has been successfully applied in many infectious disease investigations concerning seroprevalence, risk factors, time trends, etiology of disease, vaccinology, and emerging pathogens. Despite the inherent limitations of this technology, we foresee the future expansion of PhIP-Seq in both investigative studies and tracking of current, emerging, and novel viruses. Following the review of PhIP-Seq technology, its limitations, and applications, we recommend that PhIP-Seq be integrated into national surveillance programs and be used in conjunction with molecular techniques to support both One Health and pandemic preparedness efforts.

摘要

噬菌体免疫沉淀测序(PhIP-Seq)是一种高通量血清学技术,正在彻底改变我们追踪抗体谱的方式。在这篇综述中,我们主要关注其在病毒感染性疾病中的应用。通过使用表达肽段阵列的T7噬菌体下拉患者抗体,并利用下一代测序(NGS)进行检测,PhIP-Seq能够确定针对数百种蛋白质和病原体中肽段靶点的抗体库。它与传统血清学技术的不同之处在于,PhIP-Seq不需要蛋白质表达和纯化。它还允许针对整个病毒组对许多样本进行检测。PhIP-Seq已成功应用于许多关于血清流行率、危险因素、时间趋势、疾病病因、疫苗学和新出现病原体的传染病调查。尽管该技术存在固有局限性,但我们预见PhIP-Seq在调查研究以及对当前、新出现和新型病毒的追踪方面未来都会有所扩展。在对PhIP-Seq技术、其局限性和应用进行综述之后,我们建议将PhIP-Seq纳入国家监测计划,并与分子技术结合使用,以支持“同一个健康”理念和大流行防范工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daf/9143919/8cd700a4ec28/pathogens-11-00568-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daf/9143919/fbe6522edc8f/pathogens-11-00568-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daf/9143919/8cd700a4ec28/pathogens-11-00568-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daf/9143919/fbe6522edc8f/pathogens-11-00568-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daf/9143919/8cd700a4ec28/pathogens-11-00568-g001.jpg

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